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. Author manuscript; available in PMC: 2022 Jul 1.
Published in final edited form as: Lancet Diabetes Endocrinol. 2021 May 27;9(7):436–445. doi: 10.1016/S2213-8587(21)00086-3

Table 3.

Multivariable Models for Cognitive Domains*

Immediate Memory Delayed Recall Psychomotor and Mental Efficiency
β SE t-value p-value β SE t-value p-value β SE t-value p-value
Age (per 1 year) −0·015 0·003 –4·96 <0·0001 −0·013 0·004 –3·26 0·0011 −0·039 0·003 −11·70 <0·0001
Sex (men vs. women) −0·265 0·047 −5·66 <0·0001
Education (per 1 year) 0·036 0·007 5·60 <0·0001 0·042 0·008 5·05 <0·0001 0·102 0·009 11·61 <0·0001
HbA1c (per 1 %) −0·088 0·017 −5·30 <0·0001
Severe hypoglycemia (≥1 vs. 0 cumulative events) −0·178 0·040 −4·50 <0·0001
Systolic blood pressure (per 5 mm Hg) −0·013 0·003 −4·98 <0·0001
Pulse rate (per 1 bpm) −0·006 0·003 −2·22 0·027
eGFR <60 mL/min/1·73 m2 (yes vs. no)§ −0·173 0·050 −3·44 0·0008 −0·241 0·057 −4·25 <0·0001
PDR (yes vs. no)§ −0·144 0·053 −2·73 0·0067
CSME (yes vs. no)§ −0·430 0·076 −5·64 <0·0001
Confirmed clinical neuropathy (yes vs. no)§ −0·235 0·050 −4·66 <0·0001
Cardiovascular autonomic neuropathy (yes vs. no)§ −0·101 0·040 –2·50 0·013 −0·257 0·046 −5·55 <0·0001
Cardiovascular disease (yes vs. no)§ −0·293 0·069 −4·22 <0·0001
*

Data are beta coefficients, standard errors, t-values, and p-values from three separate generalized linear mixed models evaluating the association of each domain with all of the risk factors entered into the model together. With the exception of age and sex, each covariate was entered into the model as a time-dependent covariate. Covariates that did not enter into any of the three models were not included in the table. Beta estimates are equal to the difference in means between groups or the slope of the association (e.g. increase or decrease in mean domain score for every 1-unit change in the time-dependent covariate). The signed t-value corresponds to the magnitude and directionality of the association. eGFR denotes estimated glomerular filtration, PDR proliferative diabetic retinopathy, and CSME clinically-significant macular edema.

Risk factors were characterized by the time-weighted mean of all follow-up values since DCCT baseline up to each visit, weighting each value by the time interval since the last measurement.

Severe hypoglycemia was defined as events leading to coma or seizure documented by self-report for the 3-month period prior to each annual study visit. “Cumulative” refers to the running sum of all events up to each cognitive evaluation.

§

Any report between DCCT baseline and each annual study visit.